Choi Byeong Hyeok, Kim Chang Gun, Lim Yoongho, Shin Soon Young, Lee Young Han
Department of Biomedical Science and Technology, IBST, Konkuk University, Seoul 143-701, Republic of Korea.
Cancer Lett. 2008 Jan 18;259(1):111-8. doi: 10.1016/j.canlet.2007.10.003. Epub 2007 Nov 19.
Curcumin, a constituent of turmeric, has anti-inflammatory, anti-carcinogenic, and chemopreventive effects in several animal tumor models. The expression of P-glycoprotein (P-gp), encoded by the mdr gene, is often associated with multidrug resistance (MDR) to unrelated chemotherapeutic drugs in cancer cells. Here, we demonstrate that curcumin down-regulates P-gp expression in multidrug-resistant L1210/Adr cells. Transfection with a series of 5'-deleted constructs of the mdr1b gene promoter indicated that a proximal region between -205 and +42 of the sequence was responsible for the suppression of promoter activity by curcumin. This response might be associated with the inhibition of the phosphatidyinositol 3-kinase (PI3K)/Akt/nuclear factor-kappa B (NF-kappa B) signaling pathway by curcumin. Moreover, curcumin reversed the MDR of the L1210/Adr cells. Thus, curcumin can contribute to the reversal of the MDR phenotype, probably due to the suppression of P-gp expression via the inhibition of the PI3K/Akt/NF-kappa B signaling pathway.
姜黄素是姜黄的一种成分,在多种动物肿瘤模型中具有抗炎、抗癌和化学预防作用。由mdr基因编码的P-糖蛋白(P-gp)的表达通常与癌细胞对无关化疗药物的多药耐药性(MDR)相关。在此,我们证明姜黄素可下调多药耐药L1210/Adr细胞中P-gp的表达。用一系列mdr1b基因启动子的5'-缺失构建体进行转染表明,序列中-205至+42之间的近端区域负责姜黄素对启动子活性的抑制。这种反应可能与姜黄素对磷脂酰肌醇3-激酶(PI3K)/Akt/核因子-κB(NF-κB)信号通路的抑制有关。此外,姜黄素逆转了L1210/Adr细胞的多药耐药性。因此,姜黄素可能有助于逆转多药耐药表型,这可能是由于通过抑制PI3K/Akt/NF-κB信号通路来抑制P-gp的表达。